Golden har syndrome?

Ans. is 'c' i.e., 2"d & 3rd branchial arch Goldenhar syndrome (oculoauriculoveebral dysplasia with hemifacial microsomia) is a rare congenital developmental anomaly involving the first and second branchial arches. The classic features of this syndrome include ocular changes such as microphthalmia, epibulbar dermoids, lipodermoids and coloboma; aural features such as preauricular tragi, hearing loss and microtia; and veebral anomalies such as scoliosis, hemiveebrae and cervical fusion. In addition to facial, veebral, ophthalmic malformations cardiovascular, CNS, genitourinary malformations have been associated with goldenhar syndrome.